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Thoracic Epidural Analgesia in Flail Chest

Thoracic Epidural Morphine Versus Triamcinolone Acetonide Analgesia in Flail Chest

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03413059
Enrollment
40
Registered
2018-01-29
Start date
2018-02-01
Completion date
2018-07-01
Last updated
2018-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Flail Chest

Brief summary

The applicability of different thoracic epidural analgesia for patients with flail chest

Detailed description

Pain due to traumatic rib fractures may be associated with increased morbidity and mortality. Fracture ribs cause severe pain that adversely affects patients' ability to cough and breathe deeply, that may lead to decreased ventilator efforts, atelectasis, pneumonia and finally respiratory failure. That further results in longer intensive care unit (ICU) and hospital length of stay and higher mortality. Effective pain relief, chest physiotherapy and respiratory care are the points of management. Effective analgesia enables the patient to breathe deeply, cough out the secretions and comply with chest physiotherapy. Multiple pain relief treatment options are available, such as oral analgesics, intravenous opioids, patient-controlled opioid analgesia, interpleural blocks, intercostals blocks, para vertebral blocks, and epidural analgesia Recent studies reported that epidural analgesia reduces morbidity after major thoracic, abdominal and vascular surgeries, but in patients with rib fractures, Successful treatment for rib fracture pain usually requires both pharmacologic and interventional approaches .Single modality treatment, which may incite respiratory depression, is suboptimal in these patients, many of whom already manifest a compromised respiratory system. Interventional procedures, while opioid sparing, carry their own inherent risks. Intercostals nerve blocks may not be feasible in the setting of multiple rib fractures, because of patient discomfort and the risk of local aesthetic toxicity. Use of an epidural catheter with continuous infusion of local anaesthetics and opioids may pose challenges in a community hospital setting, as 24 hours in-house coverage is often unavailable. While single-shot thoracic epidural steroid injections have been used for herniated intervertebral discs, herpes zoster pain, and post herpetic neuralgia (PHN), their use in patients with rib fracture pain has not been previously reported in the literature. An epidural steroid injection delivers steroids directly into the epidural space in the spine. Sometimes additional fluid (local aesthetic and/or a normal saline solution) is used to help 'flush out' inflammatory mediators from around the area that may be a source of pain ..Typically, a solution containing cortisone (steroid) with local aesthetic (lidocaine or bupivacaine), and/or saline is used.A steroid, or cortisone, is usually injected as an anti-inflammatory agent. Inflammation is a common component of many low back conditions and reducing inflammation helps reduce pain. Triamcinolone acetonide, Dexamethasone, and Methyl prednisolone acetate are commonly used steroids.

Interventions

DRUGTriamcinolone Acetonide

thoracic epidural triamcinolone acetonide

DRUGMorphine Sulfate

Thoracic Epidural morphine

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Intervention model description

1. Group (m): which will receive morphine dose 0.1mg /kg with 9 ml of 0.125 % bupivacaine with through epidural catheter in T 7-T10 .on admission. Then continuous epidural infusion of bupivacaine (0.1 mg.kg-1.h) 2. Group (s) : will receive mixture consisting of 9 ml of 0.125 % bupivacaine with 80mg of triamcinolone ( 10 ml total volume) .through epidural catheter in-T7- T10 .on admission

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Older than 18 years. * American Society of Anesthesiologists physical status 1 or 2. * mentally competent and able to give consent for enrollment in the study

Exclusion criteria

* Patient refusal. * Psychiatric disorder * Patient younger than 18 years old * Allergy to local anesthetics, systemic opioids (fentanyl, morphine) * Impaired kidney functions and patient with coagulopathy will be also excluded. * Chronic pain syndromes and patients with chronic opioid use defined as use of regular daily doses of systemic narcotics for the past 6 months prior to the surgery. * BMI of 40 or more

Design outcomes

Primary

MeasureTime frameDescription
visual analogue score7 daysmean visual analogue score (scale of 0 to 100) indicating the severity of pain

Secondary

MeasureTime frameDescription
ICU stay7 daysfrom ICU admission to ICU discharge
chest infection7 daysincidence of developing chest infection
hospital stay7 dayslength of hospital stay

Contacts

Primary Contactmostafa H hassanein bakr, MBBCH
mostafabakr566@gmail.com+201004727908
Backup ContactEmad Z Saed, MD
Emadzarief@yahoo.com+201007046058

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026